Novel benzimidazole derivatives as selective CB2 agonists
摘要:
The preparation and evaluation of a novel class of CB2 agonists based on a benzimidazole moiety are reported. They showed binding affinities up to 1 nM towards the CB2 receptor with partial to full agonist potencies. They also demonstrated good to excellent selectivity (> 1000-fold) over the CB1 receptor. (C) 2008 Elsevier Ltd. All rights reserved.
DOI:
10.1016/j.bmcl.2008.05.073
作为产物:
描述:
4-甲氨基吡啶 、 N,N-二乙基-4-氟-3-硝基苯甲酰胺 在
crude product 、 乙酸乙酯 、 二氯甲烷 、 甲醇 作用下,
反应 87.0h,
以9:1 CH2Cl2:MeOH) to provide the title compound (0.181 g, 60%)的产率得到N,N-Diethyl-3-nitro-4-[(4-pyridinylmethyl)amino]benzamide
Compounds of general formula (I), are disclosed and claimed in the present application, as well as salts and pharmaceutical compositions comprising the novel compounds and their use in therapy, in particular in the management of pain
Compounds of general formula (I), are disclosed and claimed in the present application, as well as salts and pharmaceutical compositions comprising the novel compounds and their use in therapy, in particular in the management of pain.